EP2041074B1 - Hydrocyanation du 2-pentènenitrile - Google Patents

Hydrocyanation du 2-pentènenitrile Download PDF

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Publication number
EP2041074B1
EP2041074B1 EP07812879.0A EP07812879A EP2041074B1 EP 2041074 B1 EP2041074 B1 EP 2041074B1 EP 07812879 A EP07812879 A EP 07812879A EP 2041074 B1 EP2041074 B1 EP 2041074B1
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Prior art keywords
hydrocyanation
formula
methyl
pentenenitrile
cis
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EP2041074A2 (fr
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James Michael Garner
Christian P. Lenges
Ronald J. Mc Kinney
Wilson Tam
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Invista Technologies Sarl
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Invista Technologies SARL Switzerland
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00—Preparation of carboxylic acid nitriles
    • C07C253/08—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds
    • C07C253/10—Preparation of carboxylic acid nitriles by addition of hydrogen cyanide or salts thereof to unsaturated compounds to compounds containing carbon-to-carbon double bonds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
    • B01J31/185—Phosphites ((RO)3P), their isomeric phosphonates (R(RO)2P=O) and RO-substitution derivatives thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32—Addition reactions to C=C or C-C triple bonds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84—Metals of the iron group
    • B01J2531/847—Nickel

Definitions

  • This invention relates to the hydrocyanation of 2-pentenenitrile to produce adiponitrile and other dinitriles. More particularly, this invention relates to a process for the hydrocyanation of 2-pentenenitrile using a catalyst precursor composition comprising a zero-valent nickel and at least one bidentate phosphite ligand.
  • Hydrocyanation catalyst systems particularly pertaining to the hydrocyanation of olefins, are well known in the art.
  • systems useful for the hydrocyanation of 1,3-butadiene to form 3-pentenenitrile (3PN) and for the subsequent hydrocyanation of 3PN to form adiponitrile (ADN), are known in the commercially important nylon synthesis field.
  • the hydrocyanation of olefins using transition metal complexes with monodentate phosphite ligand is well documented in the prior art. See, for example, United States Patent Nos. 3,496,215 ; 3,631,191 ; 3,655,723 and 3,766,237 ; and Tolman, C. A., McKinney, R.
  • the hydrocyanation of activated olefins such as conjugated olefins (e.g., 1,3-butadiene and styrene) and strained olefins (e.g., norbornene) can proceed at useful rates without the use of a Lewis acid promoter.
  • unactivated olefins such as 1-octene and 3PN
  • a promoter in the hydrocyanation reaction is disclosed, for example, in United States Patent No. 3,496,217 .
  • This patent discloses an improvement in hydrocyanation using a promoter selected from a large number of metal cation compounds as nickel catalyst promoters with a wide variety of counterions.
  • United States Patent No. 3,496,218 discloses a nickel hydrocyanation catalyst promoted with various boron-containing compounds, including triphenylboron and alkali metal borohydrides.
  • United States Patent No. 4,774,353 discloses a process for the preparation of dinitriles, including ADN, from unsaturated nitriles, including pentenenitriles (PN), in the presence of a zero-valent nickel catalyst and a triorganotin promoter.
  • United States Patent No. 4,874,884 discloses a process for producing ADN by the zero-valent nickel catalyzed hydrocyanation of pentenenitriles in the presence of a synergistic combination of promoters selected in accordance with the desired reaction kinetics of the ADN synthesis. Furthermore, the use of Lewis acids to promote the hydrocyanation of pentenenitriles to produce ADN using zero-valent nickel catalysts with multidentate phosphite ligands is also disclosed. See, for example, United States Patent Nos. 5,512,696 ; 5,723,641 ; 5,959,135 ; 6,127,567 ; and 6,646,148 .
  • a recognized shortcoming of the catalyst systems and processes described above is the inability to hydrocyanate the conjugated 2-pentenenitrile isomers, 2PN.
  • United States Patent No. 3,564,040 describes that 3PN is slowly isomerized to 2PN during the hydrocyanation process, and the 2PN so produced is treated as a yield loss.
  • 2PN has been shown to be both a catalyst inhibitor and a catalyst poison as the concentration increases. In order to mitigate this poisoning effect, 2PN is typically separated before recovered pentenenitrile is recycled to the reactor.
  • United States Patent No. 3,564,040 describes a method to maintain the steady-state concentration of 2PN below 5 mole percent as based on the nitriles present in the reaction mixture. Because trans-2PN is difficult to separate from a mixture of 3PN and 4PN by distillation due to their close relative volatilities, the disclosed method involves the catalytic isomerization of trans-2PN to cis-2PN followed by fractional distillation of the mixture of PN isomers to remove the more volatile cis-2PN isomer.
  • the catalyst systems used to isomerize trans-2PN to cis-2PN are those that also serve to hydrocyanate PN to ADN, in particular, nickel catalysts derived from monodentate phosphite ligands as described in United States Patent Nos. 3,496,217 and 3,496,218 .
  • 3,852,325 are compounds of the general formula R 3 C-X, such as triphenylmethyl bromide, wherein R is an aryl radical having up to 18 carbon atoms and -X is of the group consisting of -H, -Cl, -Br, -I, -SH, -B(C 6 H 5 ) 4 , -PF 6 ,-AsF 6 , -SbF 6 and -BF 4 , while the catalyst systems described in United States Patent No. 3,852,327 are Lewis acid/Lewis base compositions, such as combinations of zinc chloride with triphenylphosphine.
  • a different method of removing the 2PN from mixtures of PN isomers containing 3PN and 4-pentenenitrile (4PN) is disclosed in United States Patent No. 3,865,865 .
  • the 2PN and/or 2-methyl-2-butenenitriles (2M2BN) can be selectively separated from a mixture of PN isomers containing 3PN and 4PN by contacting the mixture of nitriles with an aqueous solution of a treating agent comprising sulfite and bisulfite ions and ammonium or alkali metal cations to produce an aqueous phase containing the bisulfite adduct of the 2PN and/or 2M2BN and an organic phase containing the 3PN and 4PN, substantially free of 2PN or 2M2BN.
  • the recovered organic phase can provide a feed material of PN for further hydrocyanation to produce adiponitrile with greatly reduced amounts of the undesired by-product 2PN that are detrimental to catalyst efficiency.
  • hydrocyanation catalysts comprised of zero-valent nickel and a bidentate phosphite ligand have been described that are generally more active than the hydrocyanation catalyst comprised of monodentate phosphites and nickel.
  • this class of catalysts may be used effectively at much lower concentrations and over a broader range of reaction conditions.
  • United States Patent No. 5,688,986 reveals that at least one member of this class of catalysts are capable of hydrocyanating olefins conjugated to nitriles, for example 2PN.
  • this ability is not a general feature of this class of catalysts. It therefore would be desirable to identify hydrocyanation catalyst systems that can be resistant to the inhibiting and poisoning effects of 2PN.
  • EP 1 528 054 A1 discloses a process for the hydrocyanation of either 2-pentenenitrile, 3-pentenenitrile, 4-pentenenitrile, 2-methyl-3-butenenitrile or mixtures thereof in the presence of a zerovalent nickel catalyst and a promoter containing iron (II) chloride and manganese (II) chloride obtained as a byproduct from the chlorination of titanium-rich ores.
  • the nickel catalysts may be complexes of zero-valent nickel with ligands such as bidentate phosphite ligands.
  • the present invention provides a process for the hydrocyanation of 2-pentenenitrile to produce adiponitrile, comprising: contacting 2-pentenenitrile with hydrogen cyanide at a temperature in the range of 0 °C to 150 °C in the presence of at least one Lewis acid promoter and a catalyst precursor composition, wherein the catalyst precursor composition comprises a zero-valent nickel and at least one bidentate phosphite ligand selected from a member of the group represented by Formula I and Formula II, in which all like reference characters have the same meaning, except as further explicitly limited: wherein in Formula I, R 1 is isopropyl; R 2 is H; R 3 is C 1 to C 4 hydrocarbyl; R 4 is methyl; R 5 is methyl or ethyl; R 6 and R 8 are H or methyl; and R 7 is H, methyl or tertiary-butyl, and in Formula II, R 1 is is isopropyl or cyclopentyl; R 5 is methyl
  • the present invention provides a process for hydrocyanation as disclosed above, wherein the Lewis acid promoter comprises at least one compound selected from the group consisting of ZnCl 2 and FeCl 2 or a combination of such members.
  • the present invention provides a process for hydrocyanation as disclosed above, wherein the reaction temperature is in the range of 25 °C to 80 °C.
  • the present invention provides a process for hydrocyanation as disclosed above, wherein the molar ratio of the Lewis acid promoter to the nickel present in the reaction ranges from 1:10 to 10:1.
  • the present invention provides a process for hydrocyanation as disclosed above, where the catalyst precursor composition further comprises at least one monodentate phosphite ligand.
  • the invention provides a process for hydrocyanation of 2PN in the presence of at least one Lewis acid and a specified catalyst precursor composition to produce ADN.
  • the 2PN can be present in a mixture of nonconjugated unsaturated nitriles.
  • the catalyst precursor compositions of the present invention have the ability to alter the ratio of cis- and trans-2PN as well as the ability to isomerize 2PN to 3PN and 4PN in the presence of HCN.
  • the processes of the invention may comprise the use of a catalyst precursor composition that can resist the inhibiting and poisoning effects of the conjugated pentenenitrile isomer 2PN.
  • a catalyst precursor composition that can resist the inhibiting and poisoning effects of the conjugated pentenenitrile isomer 2PN.
  • the use of the broader class of catalysts, of which these bidentate phosphite ligands and catalyst precursor compositions are a subset, for the hydrocyanation of 3PN has been disclosed in United States Patent Nos. 6,127,567 and 6,171,996 .
  • ADN is of particular interest because it is a commercially versatile and important intermediate in the industrial production of nylon polyamides useful in forming films, fibers, and molded articles.
  • the term “2PN” refers to 2-pentenenitrile and 2-pentenenitriles and includes both cis-2-pentenenitrile (cis-2PN) and trans-2-pentenenitrile (trans-2PN), unless otherwise specified.
  • the term “3PN” refers to 3-pentenenitrile and 3-pentenenitriles and includes both cis-3-pentenenitrile (cis-3PN) and trans-3-pentenenitrile (trans-3PN), unless otherwise specified.
  • the term “4PN” refers to 4-pentenenitrile.
  • nonconjugated unsaturated nitriles means unsaturated nitriles other than 2PN and includes 3PN, 4PN, and nonconjugated methylbutenenitriles.
  • unsaturated nitriles includes 2PN, 3PN, 4PN, and methylbutenenitriles.
  • the 2PN useful in the present invention can be prepared by the reaction of hydrogen cyanide with 1,3-butadiene (BD).
  • BD 1,3-butadiene
  • transition metal complexes with monodentate phosphites for example, United States Patent Nos. 3,496,215 ; 3,631,191 ; 3,655,723 ; and 3,766,237
  • zero-valent nickel catalysts with multidentate phosphite ligands for example, United States Patent Nos. 5,821,378 ; 5,981,772 ; 6,020,516 ; and 6,284,865
  • the predominant pentenenitrile product formed by the hydrocyanation of BD is trans-3PN.
  • the branched BD hydrocyanation product, 2-methyl-3-butenenitrile (2M3BN) can be isomerized to trans-3PN using the same catalyst compositions employed for the hydrocyanation of BD. See, for example, United States Patent Nos. 3,536,748 and 3,676,481 .
  • the predominant trans-3PN product from the hydrocyanation of BD and isomerization of 2M3BN also contains smaller quantities of 4PN, cis-3PN, trans-2PN, cis-2PN, and 2-methyl-2-butenenitriles.
  • the 2PN useful in the present invention can be made in larger quantities during the hydrocyanation of 3PN and/or 4PN to form ADN, among other dinitriles, from the concurrent isomerization of 3PN to 2PN, as described in the prior art.
  • Separation of the cis-2PN isomer by the fractional distillation of mixtures of PN isomers, as disclosed in the art, can provide a source of isolated 2PN to be used with the present invention. See, for example, United States Patent No. 3,852,327 . 2PN produced by a different process or prepared in a separate manufacturing facility may also be used.
  • the catalyst precursor composition comprises a zero-valent nickel and at least one bidentate phosphite ligand selected from a member of the group represented by Formula I and Formula II, in which all like reference characters have the same meaning, except as further explicitly limited: wherein in Formula I, R 1 is isopropyl; R 2 is H; R 3 is C 1 to C 4 hydrocarbyl; R 4 is methyl; R 5 is methyl or ethyl; R 6 and R 8 are H or methyl; and R 7 is H, methyl or tertiary-butyl, and in Formula II, R 1 is isopropyl or cyclopentyl; R 5 is methyl or isopropyl; and R 6 , R 7 , and R 8 are H.
  • R 1 is isopropyl
  • R 2 is H
  • R 3 is C 1 to C 4 hydrocarbyl
  • R 4 is methyl
  • R 5 is methyl or ethyl
  • R 6 and R 8 are H or methyl
  • Formula I and Formula II are two-dimensional representations of three-dimensional molecules and that rotation about chemical bonds can occur in the molecules to give configurations differing from those shown.
  • rotation about the carbon-carbon bond between the 2- and 2'- positions of the biphenyl and octahydrobinaphthyl bridging groups of Formula I and Formula II, respectively can bring the two phosphorus atoms of each Formula in closer proximity to one another and can allow the phosphite ligand to bind to a single nickel atom in a bidentate fashion.
  • identityate is well known in the art and means both phosphorus atoms of the ligand are bonded to a single nickel atom.
  • hydrocarbyl is well known in the art and designates a hydrocarbon molecule from which at least one hydrogen atom has been removed. Such molecules can contain single, double, or triple bonds.
  • aryl is well known in the art and designates an aromatic hydrocarbon molecule from which at least one hydrogen atom has been removed.
  • Suitable aryl groups include those containing 6 to 10 carbon atoms, which can be unsubstituted or singly or multiply substituted.
  • Suitable substituents include, for example, C 1 -C 4 hydrocarbyl, or halogen such as fluorine, chlorine or bromine, or halogenated hydrocarbyl such a trifluoromethyl, or aryl such as phenyl.
  • Each catalyst precursor composition useful in the present invention may be considered a "precursor" composition in that the zero-valent nickel at some point becomes bound to a bidentate phosphite ligand, and further in all likelihood, additional reactions occur during hydrocyanation, such as, for example, complexing of the initial catalyst composition to an ethylenically unsaturated compound.
  • catalyst precursor composition also includes within its meaning recycled catalyst, that is, a catalyst precursor composition comprising a zero-valent nickel and at least one bidentate phosphite ligand which, having been used in the process of the invention, is returned or may be returned to the process and used again.
  • the catalyst precursor compositions may further comprise at least one monodentate phosphite ligand, provided that the monodentate phosphite ligand does not detract from the beneficial aspects of the invention.
  • the monodentate phosphite ligand may be present as an impurity from synthesis of the bidentate phosphite ligand, as disclosed in United States Patent No. 6,069,267 , or the monodentate phosphite ligand may be added as an additional component of the catalyst precursor composition.
  • the catalyst precursor compositions comprise at least one Lewis acid promoter.
  • the bidentate phosphite ligands useful in the catalyst precursor compositions employed in the present invention may be prepared by any suitable synthetic means known in the art, for example as described in United States Patent Nos. 6,171,996 , 5,512,696 , 6,069,267 , and 2004/0106815 .
  • the reaction of two equivalents of an ortho-substituted phenol with phosphorus trichloride gives the corresponding phosphorochloridite.
  • the reaction of the phosphorochloridite with the desired substituted biphenol or octahydrobinaphthol in the presence of triethylamine gives the bidentate phosphite ligand.
  • the crude bidentate phosphite ligand can be worked up by the process described in United States Patent No. 6,069,267 .
  • the bidentate phosphite ligand product mixture can typically contain the desired product in about 70% to about 90% selectivity, with other phosphite by-products such as monodentate phosphites making up the balance of the product mixture.
  • the bidentate phosphite ligand itself or these bidentate/monodentate phosphite ligand mixtures are suitable for use with the present invention.
  • the catalyst precursor compositions employed for this process should ideally be substantially free of carbon monoxide, oxygen, and water and may be preformed or prepared in situ according to techniques well known in the art.
  • the catalyst precursor composition may be formed by contacting the bidentate phosphite ligand with a zero-valent Ni complex having easily displaced ligands.
  • Ni(COD) 2 COD is 1,5-cyclooctadiene
  • COD 1,5-cyclooctadiene
  • COD tris(ortho-tolyl)phosphite
  • ethylene C 2 H 4
  • divalent nickel compounds can be combined with a reducing agent, to serve as a source of zero-valent nickel in the reaction, in the presence of the bidentate phosphite ligands of Formula I or Formula II.
  • Suitable divalent nickel compounds include compounds of the formula NiZ 2 where Z is halide, carboxylate, or acetylacetonate.
  • Suitable reducing agents include metal borohydrides, metal aluminum hydrides, metal alkyls, Li, Na, K, Zn or H 2 . See, for example, United States Patent No. 6,893,996 .
  • the bidentate phosphite ligand may be present in excess of what can theoretically be coordinated to the nickel at a given time.
  • the processes of this invention are carried out in the presence of at least one Lewis acid promoter which affects both the activity and the selectivity of the catalyst system.
  • the promoters exhibit Lewis acidity, as indicated by their ability to coordinate to either a metal-cyanide containing complex or an organonitrile, as measured spectroscopically by a shift in the infrared band assigned to the metal-cyanide or organonitrile stretch upon coordination to the promoter.
  • An example of such a spectroscopically observed shift for a soluble promoter with a nickel-cyanide (Ni-CN) species is described in Advances in Catalysis, Vol. 33 (1985), pages 12-13 .
  • the Lewis acid promoters may comprise an inorganic or organometallic compound in which the cation is selected from the group consisting of scandium, titanium, vanadium, chromium, manganese, iron, cobalt, copper, zinc, boron, aluminum, yttrium, zirconium, niobium, molybdenum, cadmium, rhenium, lanthanum, erbium, ytterbium, samarium, tantalum, and tin, as is well-known in the art.
  • Lewis acid promoters include, but are not limited to BPh 3 , ZnBr 2 , Znl 2 , ZnCl 2 , ZnSO 4 , CuCl 2 , CuCl, Cu(O 3 SCF 3 ) 2 , CoCl 2 , Col 2 , Fel 2 , FeCl 3 , FeCl 2 , FeCl 2 (THF) 2 , TiCl 2 , TiCl 4 (THF) 2 , MnCl 2 , ScCl 3 , AlCl 3 , (C 8 H 17 )AlCl 2 , (C 8 H 17 ) 2 AlCl, (iso-C 4 H 9 ) 2 AlCl, Ph 2 AlCl, PhAlCl 2 , ReCl 5 , ZrCl 4 , NbCl 5 , VCl 3 , CrCl 2 , MoCl 5 , YCl 3 , CdCl 2 , LaCl 3 ,
  • the catalyst precursor composition may be dissolved in a solvent that is non-reactive toward, and miscible with, the hydrocyanation reaction mixture.
  • suitable solvents include, for example, aliphatic and aromatic hydrocarbons with 1 to 10 carbon atoms and nitrile solvents such as acetonitrile.
  • 3PN a mixture of isomeric pentenenitriles, a mixture of isomeric methylbutenenitriles, a mixture of isomeric pentenenitriles and isomeric methylbutenenitriles, or the reaction product from a previous reaction campaign may be used to dissolve the catalyst precursor composition.
  • the processes of the invention can be carried out with or without a solvent.
  • the solvent should be liquid at the reaction temperature and pressure, and should be inert towards the 2PN and the catalyst.
  • solvents include hydrocarbons such as benzene or xylene, or nitriles such as 3PN, acetonitrile or benzonitrile.
  • the processes of the invention are carried out at a temperature range from 0 °C to 150 °C, for example from 25 °C to 80 °C.
  • atmospheric pressure is suitable for carrying out the processes of the invention
  • higher and lower pressures can be used.
  • pressures of from about 0.05 to about 10 atmospheres (about 5.0 to about 1013 kPa) may be used.
  • Higher pressures, up to about 10,000 kPa or more, can be used, if desired, but any benefit that may be obtained thereby may not be justified in view of increased cost of such operations.
  • the overall feed molar ratio of HCN to zero-valent nickel may, for example, be in the range of about 100:1 to about 3000:1, for example in the range of about 300:1 to about 2000:1.
  • the reaction vessel may be partially charged, for example, with either a solution of a catalyst precursor composition in substrate pentenenitriles or the reactor product from a previous reaction campaign, followed by initiation of all reactor feeds. Continuous reactor product removal may begin upon establishing the desired fluid levels within the reaction vessel or vessels.
  • HCN substantially free of carbon monoxide, oxygen, ammonia, and water can be introduced to the reaction as a vapor, liquid, or mixtures thereof.
  • a cyanohydrin can be used as the source of HCN. See, for example, United States Patent No. 3,655,723 .
  • the reaction medium may be agitated, such as by stirring or shaking.
  • mixing of the reactants and the reaction mixture may be achieved through any means well known in the art that provides mass transfer sufficient to avoid areas of high and/or low reactant concentrations in the reaction mixture.
  • the reaction product and components of the catalyst precursor composition can be recovered by conventional techniques known in the art, such as, for example, by liquid-liquid extraction as disclosed in United States Patent No. 6,936,171 , and by distillation.
  • the reaction may be run in batch, semi-continuous, or continuous manners.
  • Isomerization of 2PN to 3PN and 4PN in the presence of HCN can be useful in that it can provide the desired 3PN and 4PN isomers, which may be hydrocyanated to form ADN. Additionally, isomerization of 2PN to other PN isomers can be advantageous in that the amount of inhibiting 2PN is reduced. Alteration of the ratio of cis-2PN to trans-2PN can also be advantageous by enabling the purge of cis-2PN from pentenenitrile mixtures. In this way, 2PN can be purged from the 3PN, 4PN, and catalyst mixture which is recycled to the hydrocyanation reactor, and the build-up of 2PN is avoided.
  • Cis-2-pentenenitrile (98%) produced from a 1,3-butadiene and 3PN hydrocyanation process may be obtained commercially from the Sigma-Aldrich Chemical Company.
  • Hydroperoxide impurities can be common in such a reagent and are typically detrimental to hydrocyanation catalyst performance. Hydroperoxide impurities can be measured and reduced in cis-2PN, if necessary, by titration, for example with triphenylphosphine, prior to purification by distillation.
  • Distillation under a nitrogen atmosphere can be utilized to remove the majority of oxygen, water, and peroxides and heavy boilers by taking, for example, a forecut and a heartcut during the distillation.
  • the purified cis-2PN of the heartcut can be transferred into a drybox filled with an inert gas such as nitrogen and can be dried further over 3A molecular sieves (which have been previously dried and degassed under nitrogen).
  • a toluene solution of a ligand of Formula I or Formula II (0.230 mL of 0.21 mol ligand/L of toluene) was treated with Ni(COD) 2 solution (0.320 mL) and thoroughly mixed to provide a catalyst precursor solution.
  • a cis-2-pentenenitrile (cis-2PN)/ZnCl 2 solution was prepared by dissolving ZnCl 2 (0.017 g in 1.02 g cis-2PN).
  • a sample of catalyst solution (0.100 mL) was treated with cis-2PN/ZnCl 2 solution (0.025 mL); and the mixture heated to 50 °C. From a liquid, uninhibited, anhydrous HCN sample at ambient temperature, HCN vapor was continuously delivered to the reaction mixture over a period of 16 hours.
  • ADN adiponitrile
  • MGN 2-methylglutaronitrile
  • ESN 2-ethylsuccinonitrile
  • Table I reports the percentage of cis-2PN that was converted to dinitriles (ADN+MGN+ESN). In every case ADN comprised greater than 90% of the dinitriles produced.
  • n-C3H7 is normal-propyl
  • i-C3H7 is iso-propyl
  • n-C4H9 is normal-butyl
  • n-Butyl is normal-butyl
  • sec-C4H9 is secondary-butyl
  • t-C4H9 is tertiary-butyl groups.
  • a toluene solution of a ligand of Formula I or II was treated with the Ni(COD) 2 solution and thoroughly mixed to provide a catalyst precursor solution.
  • a cis-2PN/promoter solution was prepared by dissolving the appropriate promoter in cis-2PN.
  • a sample of catalyst solution was treated with the cis-2PN/promoter solution, and the mixture adjusted to the reaction temperature.
  • HCN vapor was continuously delivered to the 2PN catalyst solution from a liquid, uninhibited, anhydrous HCN sample at ambient temperature. The specified temperature was maintained during the reaction period.
  • ADN adiponitrile
  • MGN 2-methylglutaronitrile
  • ESN 2-ethylsuccinonitrile
  • Table II reports the percentage of cis-2PN that was converted to dinitriles (ADN+MGN+ESN). In every case, ADN comprised greater than 90% of the dinitriles produced.
  • the molar ratio of Ni to cis-2PN was 1 to 200.
  • the molar ratio of promoter to Ni was 3 to 1.
  • the molar ratio of ligand to Ni was 3 to 1.
  • the reaction was carried out at 25 °C for 95 hours.
  • the molar ratio of Ni to cis-2PN was 1 to 67.
  • the molar ratio of promoter to Ni was 1 to 1.
  • the molar ratio of ligand to Ni was 3 to 1.
  • the reaction was carried out at 50 °C for 6 hours.
  • Example 56 the molar ratio of Ni to cis-2PN was 1 to 67.
  • the molar ratio of promoter to Ni was 3 to 1.
  • the molar ratio of ligand to Ni was 3 to 1.
  • the reaction was carried out at 25 °C for 70 hours.
  • Example 57 the molar ratio of Ni to cis-2PN was 1 to 200.
  • the molar ratio of promoter to Ni was 1 to 1.
  • the molar ratio of ligand to Ni was 3 to 1.
  • the reaction was carried out at 50 °C for 70 hours.
  • the molar ratio of Ni to cis-2PN was 1 to 67.
  • the molar ratio of promoter to Ni was 3 to 1.
  • the molar ratio of ligand to Ni was 3 to 1.
  • the reaction was carried out at 25 °C for 72 hours.
  • the molar ratio of Ni to cis-2PN was 1 to 67.
  • the molar ratio of promoter to Ni was 3 to 1.
  • the molar ratio of ligand to Ni was 3 to 1.
  • the reaction was carried out at 25 °C for 72 hours.
  • Example 65 the molar ratio of Ni to cis-2PN was 1 to 200.
  • the molar ratio of promoter to Ni was 1 to 1.
  • the molar ratio of ligand to Ni was 2 to 1.
  • the reaction was carried out at 50 °C for 6 hours.
  • the molar ratio of Ni to cis-2PN was 1 to 67.
  • the molar ratio of promoter to Ni was 3 to 1.
  • the molar ratio of ligand to Ni was 3 to 1.
  • the reaction was carried out at 25 °C for 72 hours.

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Claims (5)

  1. Procédé d'hydrocyanation du 2-pentènenitrile pour produire de l'adiponitrile, comprenant:
    la mise en contact du 2-pentènenitrile avec du cyanure d'hydrogène à une température se situant dans la plage de 0 à 150 °C en présence d'au moins un promoteur d'acide de Lewis et d'une composition de précurseur de catalyseur, dans lequel la composition de précurseur de catalyseur comprend un nickel à valence zéro et au moins un ligand de phosphite bidenté sélectionné parmi les membres du groupe représenté par les formules I et II, dans lesquelles toutes les lettres de référence ont la même signification, sauf précision contraire :
    Figure imgb0008
    dans lequel, dans la formule I, R1 représente un groupe isopropyle ; R2 représente H ; R3 représente un groupe hydrocarbyle en C1 à C4 ; R4 représente un groupe méthyle ;
    R5 représente un groupe méthyle ou éthyle ; R6 et R8 représentent H ou un groupe méthyle ; et R7 représente H, un groupe méthyle ou butyle tertiaire, et dans la formule II, R1 représente un groupe isopropyle ou cyclopentyle ; R5 représente un groupe méthyle ou isopropyle ; et R6, R7 et R8 représentent H.
  2. Procédé selon la revendication 1, dans lequel le promoteur d'acide de Lewis comprend au moins un composé sélectionné dans le groupe constitué de ZnCl2 et FeCl2 ou d'une combinaison desdits éléments.
  3. Procédé selon la revendication 1, dans lequel la température réactionnelle se situe dans la plage de 25 à 80 °C.
  4. Procédé selon la revendication 1, dans lequel le rapport molaire entre le promoteur d'acide de Lewis et le nickel présent dans la réaction varie de 1/10 à 10/1.
  5. Procédé selon l'une quelconque des revendications 1 à 4, dans lequel la composition de précurseur de catalyseur comprend, en outre, au moins un ligand de phosphite monodenté.
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WO2008008927A2 (fr) 2008-01-17
CN101479237A (zh) 2009-07-08
CN105017071A (zh) 2015-11-04
BRPI0713247A2 (pt) 2012-04-17
EP2041074A2 (fr) 2009-04-01
RU2009105095A (ru) 2010-08-27
JP2009543880A (ja) 2009-12-10
US20080015379A1 (en) 2008-01-17
SA07280379B1 (ar) 2011-09-13
US20120035387A1 (en) 2012-02-09
US8394981B2 (en) 2013-03-12
US7919646B2 (en) 2011-04-05

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